Ibuprofen
- Product NDC
- 37808-221
- 11-digit product format
- 378080221
- Labeler code
- 37808
- Product ID
- 37808-221_2227b10d-117f-49e0-839d-106f10498f66
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ibuprofen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA202300
- Marketing category
- ANDA
- Marketing start
- 2018-03-31
- Marketing end
- 0000-00-00
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-221 | IBUPROFEN CAPSULE, LIQUID FILLED [H E B] | 4 | Legacy NDC | 20230213_e809e675-2f81-4b8a-b33e-b63c88600cd8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-221-20 | 37808022120 | 1 BOTTLE, PLASTIC in 1 BOX (37808-221-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2018-03-31 | 0000-00-00 | No | No | Current |
| 37808-221-30 | 37808022130 | 300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (37808-221-30) | 2018-03-31 | 0000-00-00 | No | No | Current |
| 37808-221-40 | 37808022140 | 1 BOTTLE, PLASTIC in 1 BOX (37808-221-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC | 2018-03-31 | 0000-00-00 | No | No | Current |
| 37808-221-80 | 37808022180 | 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (37808-221-80) | 2018-03-31 | 0000-00-00 | No | No | Current |